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A Retrospective Analysis of the Clinical Effectiveness of Tigecycline in the Treatment of Clostridioides difficile -Associated Diarrhea.

Authors :
Johannesmeyer, Herman Joseph
Baloyan, Luiza
Kolyouthapong, Kristica
Source :
Pharmacoepidemiology (2813-0618). Jun2024, Vol. 3 Issue 2, p231-240. 10p.
Publication Year :
2024

Abstract

Clostridioides difficile infection (CDI) is the leading cause of nosocomial diarrhea in the United States. Tigecycline has been proposed as a potential treatment for CDI, though limited clinical data exist to support this practice. The objective of this study was to determine if the provision of tigecycline provides a clinically meaningful benefit to inpatients with CDI. This study was a retrospective chart review enrolling inpatients receiving treatment for CDI. Patients were divided into cohorts depending on whether they received a standard antibiotic therapy regimen for CDI or an antibiotic treatment regimen that included tigecycline. The primary outcome was clinical recovery at the time of hospital discharge. A total of 39 and 22 patients were included in the standard antibiotic therapy and tigecycline groups, respectively. ATLAS (Age, Treatment, Leukocyte, Albumin, Serum creatinine) scores at the time of CDI diagnosis were similar between the two groups, though patients in the tigecycline groups were more likely to represent a recurrent episode of CDI. There was no difference in the rate of clinical recovery at the time of hospital discharge between the standard antibiotic therapy and tigecycline groups (38.5% vs. 36.4%, p = 0.8710). These data do not support the routine use of tigecycline for the treatment of CDI, though interpretation is limited due to baseline differences between groups and the retrospective, observational nature of this study. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
28130618
Volume :
3
Issue :
2
Database :
Academic Search Index
Journal :
Pharmacoepidemiology (2813-0618)
Publication Type :
Academic Journal
Accession number :
178183919
Full Text :
https://doi.org/10.3390/pharma3020015